所有图片(4)
About This Item
线性分子式:
CH3(CH2)15OH
CAS号:
分子量:
242.44
Beilstein:
1748475
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
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蒸汽密度
8.34 (vs air)
蒸汽壓力
<0.01 mmHg ( 43 °C)
產品線
ReagentPlus®
化驗
99%
形狀
solid
自燃溫度
483 °F
expl. lim.
8 %
bp
179-181 °C/10 mmHg (lit.)
mp
48-50 °C (lit.)
溶解度
ethanol: soluble 100 mL/mL, clear to very slightly hazy, colorless
密度
0.818 g/mL at 25 °C (lit.)
SMILES 字串
CCCCCCCCCCCCCCCCO
InChI
1S/C16H34O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17/h17H,2-16H2,1H3
InChI 密鑰
BXWNKGSJHAJOGX-UHFFFAOYSA-N
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一般說明
1-十六醇是一种脂肪醇，用于表面活性剂、润滑剂、去污剂、药物和化妆品中。
應用
1-十六醇已用于制备：
- (±)-2-甲氧基十七烷酸（脂肪酸）
- 1-十六烷醇的高链脂肪酸酯，用于热能储存的新型有机相变材料
- 十六烷（烷烃）存在于弗尼斯弧菌 M1 膜组分中
法律資訊
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
nwg
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
其他客户在看
Metabolic engineering of Saccharomyces cerevisiae to produce 1-hexadecanol from xylose
Guo, et al.
Microbial cell factories, 15, 1-11 (2016)
Néstor M Carballeira et al.
Pure and applied chemistry. Chimie pure et appliquee, 84(9), 1867-1875 (2012-11-03)
The fatty acids (±)-2-methoxy-6Z-heptadecenoic acid (1), (±)-2-methoxy-6-heptadecynoic acid (2) and (±)-2-methoxyheptadecanoic acid (3) were synthesized and their inhibitory activity against the Leishmania DNA topoisomerase IB enzyme (LdTopIB) determined. Acids 1 and 2 were synthesized from 4-bromo-1-pentanol, the former in ten
Metabolic engineering of Saccharomyces cerevisiae to improve 1-hexadecanol production
Feng, et al.
Metabolic engineering, 27, 10-19 (2015)
High-chain fatty acid esters of 1-hexadecanol for low temperature thermal energy storage with phase change materials.
Aydin AA and Aydin A.
Solar Energy Mat. and Solar Cells, 96, 93-100 (2012)
Myong-Ok Park
Journal of bacteriology, 187(4), 1426-1429 (2005-02-03)
Alkane biosynthesis in the bacterium Vibrio furnissii M1 involves the synthesis of long-chain alkanes via 1-alcohol. Evidence for this novel pathway are the following. (i) Both even- and odd-carbon-number n-alkanes were produced from glucose, while only even-carbon-number fatty acids were
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